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Water coordinated on Cu(I)-based catalysts is the oxygen source in CO2 reduction to CO.


ABSTRACT: Catalytic reduction of CO2 over Cu-based catalysts can produce various carbon-based products such as the critical intermediate CO, yet significant challenges remain in shedding light on the underlying mechanisms. Here, we develop a modified triple-stage quadrupole mass spectrometer to monitor the reduction of CO2 to CO in the gas phase online. Our experimental observations reveal that the coordinated H2O on Cu(I)-based catalysts promotes CO2 adsorption and reduction to CO, and the resulting efficiencies are two orders of magnitude higher than those without H2O. Isotope-labeling studies render compelling evidence that the O atom in produced CO originates from the coordinated H2O on catalysts, rather than CO2 itself. Combining experimental observations and computational calculations with density functional theory, we propose a detailed reaction mechanism of CO2 reduction to CO over Cu(I)-based catalysts with coordinated H2O. This study offers an effective method to reveal the vital roles of H2O in promoting metal catalysts to CO2 reduction.

SUBMITTER: Zheng Y 

PROVIDER: S-EPMC9095693 | biostudies-literature | 2022 May

REPOSITORIES: biostudies-literature

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Water coordinated on Cu(I)-based catalysts is the oxygen source in CO<sub>2</sub> reduction to CO.

Zheng Yajun Y   Yao Hedan H   Di Ruinan R   Xiang Zhicheng Z   Wang Qiang Q   Lu Fangfang F   Li Yu Y   Yang Guangxing G   Ma Qiang Q   Zhang Zhiping Z  

Nature communications 20220511 1


Catalytic reduction of CO<sub>2</sub> over Cu-based catalysts can produce various carbon-based products such as the critical intermediate CO, yet significant challenges remain in shedding light on the underlying mechanisms. Here, we develop a modified triple-stage quadrupole mass spectrometer to monitor the reduction of CO<sub>2</sub> to CO in the gas phase online. Our experimental observations reveal that the coordinated H<sub>2</sub>O on Cu(I)-based catalysts promotes CO<sub>2</sub> adsorption  ...[more]

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